EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
3.1.1.57 | Sphingobium sp. | O87170 | - |
- |
3.1.1.57 | Sphingobium sp. NBRC 103272 | O87170 | - |
- |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
3.1.1.57 | 2-oxo-2H-pyran-4,6-dicarboxylate + H2O | - |
Sphingobium sp. | (1E)-4-oxobut-1-ene-1,2,4-tricarboxylate | - |
? | |
3.1.1.57 | 2-oxo-2H-pyran-4,6-dicarboxylate + H2O | - |
Sphingobium sp. NBRC 103272 | (1E)-4-oxobut-1-ene-1,2,4-tricarboxylate | - |
? | |
3.1.1.57 | additional information | the catalytic reaction contains the nucleophilic attack, the cleavage of C-O bond of lactone (substrate) and the intramolecular proton transfer. The intermediate has two intramolecular proton transfer pathways, leading to two final hydrolysis products. According to the energy profile, 4-carboxy-2-hydroxymuconate is the main hydrolysis product, and the isomerization between 4-carboxy-2-hydroxymuconate and 4-oxalomesaconate is suggested to occur in solvent. Residue Asp248 acts as a general base to activate the hydrolytic water molecule. Residues His31, His33 and His180 play assistant roles | Sphingobium sp. | ? | - |
? | |
3.1.1.57 | additional information | the catalytic reaction contains the nucleophilic attack, the cleavage of C-O bond of lactone (substrate) and the intramolecular proton transfer. The intermediate has two intramolecular proton transfer pathways, leading to two final hydrolysis products. According to the energy profile, 4-carboxy-2-hydroxymuconate is the main hydrolysis product, and the isomerization between 4-carboxy-2-hydroxymuconate and 4-oxalomesaconate is suggested to occur in solvent. Residue Asp248 acts as a general base to activate the hydrolytic water molecule. Residues His31, His33 and His180 play assistant roles | Sphingobium sp. NBRC 103272 | ? | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
3.1.1.57 | LigI | - |
Sphingobium sp. |